Hereditary hyperbilirubinemia

rare

An inherited disorder affecting the metabolism of bilirubin. It results in increased levels of bilirubin in the blood. Representative examples of this condition include Gilbert syndrome and Crigler-Najjar syndrome.

Identifiers: MONDO:0002408
Part of: Hyperbilirubinemia Inborn disorder of bilirubin metabolism

Subtypes

All diseases Rare only

Disease	ID	Subtypes	Genes
Crigler-Najjar syndrome	MONDO:0009044	2
Dubin-Johnson syndrome	MONDO:0009380		ABCC2
Gilbert syndrome	MONDO:0007745		UGT1A1
Rotor syndrome	MONDO:0009379
Hyperbilirubinemia, conjugated, type 3	MONDO:0009381
Hyperbilirubinemia, shunt, primary	MONDO:0009382
Transient familial neonatal hyperbilirubinemia	MONDO:0009383		UGT1A1

Rare disease

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